Golgi reassembly after mitosis: the AAA family meets the ubiquitin family.

Biochimica et biophysica acta Pub Date : 2005-07-10
Hemmo H Meyer
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Abstract

The Golgi apparatus in animal cells breaks down at the onset of mitosis and is later rebuilt in the two daughter cells. Two AAA ATPases, NSF and p97/VCP, have been implicated in regulating membrane fusion steps that lead to regrowth of Golgi cisternae from mitotic fragments. NSF dissociates complexes of SNARE proteins, thereby reactivating them to mediate membrane fusion. However, NSF has a second function in regulating SNARE pairing together with the ubiquitin-like protein GATE-16. p97/VCP, on the other hand, is involved in a cycle of ubiquitination and deubiquitination of an unknown target that governs Golgi membrane dynamics. Here, these findings are reviewed and discussed in the context of the increasingly evident role of ubiquitin in membrane traffic processes.

有丝分裂后高尔基重组:AAA家族与泛素家族相遇。
动物细胞中的高尔基体在有丝分裂开始时分解,随后在两个子细胞中重建。两个AAA atp酶NSF和p97/VCP参与调节膜融合步骤,导致高尔基池从有丝分裂片段中再生。NSF解离SNARE蛋白复合物,从而重新激活它们介导膜融合。然而,NSF的第二个功能是调节SNARE与泛素样蛋白GATE-16的配对。另一方面,p97/VCP参与控制高尔基膜动力学的未知靶点的泛素化和去泛素化循环。在此,这些发现在泛素在膜运输过程中日益明显的作用的背景下进行了回顾和讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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